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BACKGROUND: Inherited retinal degenerations are a major cause of untreatable blindness in the younger age group. Recent advances in gene therapy using adeno-associated viral (AAV) vectors have raised the possibility of slowing or stopping retinal degenerations with gene replacement in cases of gene deficiency. MATERIALS AND METHODS: In this report, we present a family with autosomal dominant retinitis pigmentosa. A screen for common ADRP genes was performed with 105 genes targeted. Next generation sequencing was used to identify the mutation which was next confirmed by bidirectional Sanger sequencing. RESULTS: A novel mutation of the TOPORS gene was identified, c.2539C>T p.(Arg847Ter), resulting in a premature termination codon and suggesting haploinsufficiency as the pathological mechanism. CONCLUSIONS: Since the cDNA encoding TOPORS is 3,135 nucleotides (within the coding capacity of AAV vectors) and haploinsufficiency is a mechanism relating to inadequate gene expression, gene replacement therapy may be an option for patients with this condition.

Original publication

DOI

10.1080/13816810.2017.1313994

Type

Journal article

Journal

Ophthalmic Genet

Publication Date

12/2017

Volume

38

Pages

562 - 566

Keywords

Autosomal dominant retinitis pigmentosa, TOPORS gene, haploinsufficiency, Adult, Codon, Nonsense, DNA Mutational Analysis, Female, Genes, Dominant, Haploinsufficiency, High-Throughput Nucleotide Sequencing, Humans, Middle Aged, Mutation, Neoplasm Proteins, Nuclear Proteins, Pedigree, Retinitis Pigmentosa, Ubiquitin-Protein Ligases